Effect of CS1 in Subjects With Pulmonary Arterial Hypertension

PHASE2CompletedINTERVENTIONAL
Enrollment

25

Participants

Timeline

Start Date

May 5, 2022

Primary Completion Date

August 1, 2024

Study Completion Date

August 1, 2024

Conditions
Pulmonary Arterial Hypertension
Interventions
DRUG

CS1 Administration

CS1 delayed-release capsules will be supplied with 160 mg active pharmaceutical ingredient (sodium valproate) per capsule. Three dose levels that will be evaluated in this study; study drug will be administered as uneven, divided doses twice daily in the morning and in the evening (1/3 of the daily dose is to be administered between 7 and 9 am; 2/3 of the daily dose is to be administered between 7 and 9 pm).

Trial Locations (1)

Unknown

Fredrik Frick, Gothenburg

Sponsors
All Listed Sponsors
collaborator

Worldwide Clinical Trials

OTHER

lead

Cereno Scientific AB

INDUSTRY